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AB24233

Anti-MC4-R antibody

4

(18 Reviews)

|

(27 Publications)

Rabbit Polyclonal MC4-R antibody. Suitable for WB, IHC-P and reacts with Human, Rat samples. Cited in 27 publications. Immunogen corresponding to Synthetic Peptide within Mouse Mc4r aa 1-50.

View Alternative Names

Melanocortin receptor 4, MC4-R, MC4R

2 Images
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MC4-R antibody (AB24233)
  • IHC-P

Unknown

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MC4-R antibody (AB24233)

Immunoperoxidase staining of rat brain section with ab24233. Note the tadpole like staining of cortex neurons.

Western blot - Anti-MC4-R antibody (AB24233)
  • WB

Unknown

Western blot - Anti-MC4-R antibody (AB24233)

All lanes:

Western blot - Anti-MC4-R antibody (ab24233)

Lane 1:

Human cerebella cortex pellet. at 30 µg

Lane 2:

Human hippocampus homogenate. at 30 µg

Predicted band size: 36 kDa

Observed band size: 55 kDa

false

Key facts

Host species

Rabbit

Clonality

Polyclonal

Isotype

IgG

Carrier free

No

Reacts with

Rat, Human

Applications

WB, IHC-P

applications

Immunogen

Synthetic Peptide within Mouse Mc4r aa 1-50. The exact immunogen used to generate this antibody is proprietary information.

P56450

Reactivity data

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Product details

This antibody mainly detects an unglycosylated protein at 37kDa and a glycosylated protein at 55kDa.

Properties and storage information

Form
Liquid
Purification technique
Affinity purification Protein A
Storage buffer
pH: 7.4 Preservative: 0.02% Sodium azide Constituents: Tris buffered saline, 50% Glycerol (glycerin, glycerine), 0.1% BSA
Shipped at conditions
Blue Ice
Appropriate short-term storage duration
1-2 weeks
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
-20°C
Aliquoting information
Upon delivery aliquot
Storage information
Avoid freeze / thaw cycle

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

The melanocortin-4 receptor also known as MC4-R is a G protein-coupled receptor found within the melanocortin receptor family. It has a molecular mass of approximately 38 kDa. MC4-R is expressed in the central nervous system with high levels in the hypothalamus a region that regulates energy balance and homeostasis. The receptor is activated by several peptide ligands including alpha-melanocyte-stimulating hormone (α-MSH) and it interacts with specific signaling cascades through G proteins.
Biological function summary

The actions through MC4-R are important for energy regulation and appetite control. As part of the melanocortin system MC4-R influences feeding behavior and energy expenditure. Its activation by endogenous or synthetic MC4-R activators suppresses appetite and increases energy consumption. The receptor does not work alone; it forms part of a signaling complex involving other receptor proteins such as MC3-R. The activity of MC4-R also connects to the regulation of body weight and influences fat mass.

Pathways

MC4-R plays an important role in the leptin-melanocortin pathway and the central regulation of energy homeostasis. Leptin a hormone produced by adipose tissues acts upstream by enhancing α-MSH production which in turn activates MC4-R. This activation leads to reduced food intake and increased thermogenesis. Moreover MC4-R interacts with another important signaling protein AGRP (Agouti-related peptide) which acts as an antagonist opposing the effects of α-MSH and regulating energy balance in a complex feedback system.

Mutations or dysregulation of MC4-R are linked to obesity and metabolic syndrome. About 5% of severe early-onset obesity cases involve mutations in the MC4-R gene. The receptor influences the risk for obesity-related conditions through its interactions with AGRP and α-MSH. Additionally compromised MC4-R signaling can lead to disorders such as cachexia where it impacts appetite and metabolism related to conditions like cancer or chronic illness. Defective MC4-R activity therefore is important in understanding the intricate balance between appetite energy expenditure and body mass control.

Product protocols

For this product, it's our understanding that no specific protocols are required. You can visit:

Target data

G protein-coupled receptor that binds melanocyte-stimulating hormones (alpha- and beta-MSH) and corticotropin/ACTH, which are peptide products of the POMC precursor (PubMed : 12646665, PubMed : 14764818, PubMed : 25163632, PubMed : 32327598, PubMed : 33858992, PubMed : 8392067). Functions as a central component of the leptin-melanocortin pathway, which is essential for maintaining energy homeostasis (PubMed : 32327598, PubMed : 33858992). Upon activation, couples to G(s) protein, stimulating adenylate cyclase and the cAMP-dependent signaling pathway, which promotes anorexogenic signaling in the hypothalamus and contributes to a negative energy balance (PubMed : 12588803, PubMed : 14764818, PubMed : 25163632, PubMed : 33858992). Regulates food intake : activation by agonists suppresses appetite, whereas the antagonist Agouti-related protein/AGRP precludes agonist-induced signaling, thereby stimulating appetite (PubMed : 9311920). Modulates the firing activity of neurons in paraventricular nucleus (PVN) of the hypothalamus via alpha-MSH and AGRP regulation of inwardly rectifying potassium channel KCNJ13 closure, independently of G(s) signaling (PubMed : 32327598). In the PVN, also interacts with opsin 3/OPN3, which couples to G(i/o) proteins to inhibit MC4R-mediated cAMP signaling, thereby promoting food intake (PubMed : 39951488). In intestinal epithelial cells, contributes to inhibition of hepatic glucose production via nesfatin-1/NUCB2, leading to increased cAMP levels and glucagon-like peptide 1 (GLP-1) secretion (PubMed : 39562740). Interaction with MGRN1 displaces the G(s) protein, further decreasing MC4R signaling activity (PubMed : 19737927). Also activated by gamma-MSH, though with low potency (PubMed : 8392067).
See full target information MC4R

Publications (27)

Recent publications for all applications. Explore the full list and refine your search

The EMBO journal 44:54-74 PubMed39562740

2024

Intestinal NUCB2/nesfatin-1 regulates hepatic glucose production via the MC4R-cAMP-GLP-1 pathway.

Applications

Unspecified application

Species

Unspecified reactive species

Shan Geng,Shan Yang,Xuejiao Tang,Shiyao Xue,Ke Li,Dongfang Liu,Chen Chen,Zhiming Zhu,Hongting Zheng,Yuanqiang Wang,Gangyi Yang,Ling Li,Mengliu Yang

FASEB journal : official publication of the Federation of American Societies for Experimental Biology 37:e23274 PubMed37917004

2023

GRP78 acts as a cAMP/PKA signaling modulator through the MC4R pathway in porcine embryonic development.

Applications

Unspecified application

Species

Unspecified reactive species

Geun Heo,Song-Hee Lee,Ji-Dam Kim,Gyu-Hyun Lee,Jae-Min Sim,Dongjie Zhou,Jing Guo,Xiang-Shun Cui

Scientific reports 13:12666 PubMed37542065

2023

Increased body weight in mice with fragile X messenger ribonucleoprotein 1 (Fmr1) gene mutation is associated with hypothalamic dysfunction.

Applications

Unspecified application

Species

Unspecified reactive species

Rebecca E Ruggiero-Ruff,Pedro A Villa,Sarah Abu Hijleh,Bryant Avalos,Nicholas V DiPatrizio,Sachiko Haga-Yamanaka,Djurdjica Coss

FASEB journal : official publication of the Federation of American Societies for Experimental Biology 37:e22920 PubMed37078546

2023

Glutamatergic melanocortin-4 receptor neurons regulate body weight.

Applications

Unspecified application

Species

Unspecified reactive species

Haodong Liu,Xiaojing Li,Penghui Li,Rihan Hai,Jiacheng Li,Qi Fan,Xing Wang,Yujie Chen,Xiaojuan Cao,Xiaoyu Zhang,Ruifeng Gao,Kun Wang,Chenguang Du

Frontiers in endocrinology 14:983670 PubMed37033219

2023

Melanocortin 4 receptor signaling in Sim1 neurons permits sexual receptivity in female mice.

Applications

Unspecified application

Species

Unspecified reactive species

Erin A Semple,Mitchell T Harberson,Baijie Xu,Rebecca Rashleigh,Tori L Cartwright,Jessica J Braun,Amy C Custer,Chen Liu,Jennifer W Hill

Science advances 9:eadd5330 PubMed36791202

2023

A gut-brain axis mediates sodium appetite via gastrointestinal peptide regulation on a medulla-hypothalamic circuit.

Applications

Unspecified application

Species

Unspecified reactive species

Yuchu Liu,Ji-An Wei,Zhihua Luo,Jing Cui,Yifan Luo,Sarah Oi Kwan Mak,Siqi Wang,Fengwei Zhang,Yan Yang,Kwok-Fai So,Lingling Shi,Li Zhang,Billy Kwok Chong Chow

The Journal of biological chemistry 299:102728 PubMed36410433

2022

rAAV-CRISPRa therapy corrects Rai1 haploinsufficiency and rescues selective disease features in Smith-Magenis syndrome mice.

Applications

Unspecified application

Species

Unspecified reactive species

Hao-Cheng Chang,Yu-Ju Lee,Sehrish Javed,Minza Haque,Ya-Ting Chang,Yu Cheng Lin,Cameron Oram,Wei-Hsiang Huang

Biomedicines 10: PubMed36289871

2022

Obesity-Related Genes Expression in Testes and Sperm Parameters Respond to GLP-1 and Caloric Restriction.

Applications

Unspecified application

Species

Unspecified reactive species

Ana S Correia,Sara C Pereira,Tiago Morais,Ana D Martins,Mariana P Monteiro,Marco G Alves,Pedro F Oliveira

Sleep 44: PubMed33624805

2021

Leptin receptor expression in the dorsomedial hypothalamus stimulates breathing during NREM sleep in db/db mice.

Applications

Unspecified application

Species

Unspecified reactive species

Huy Pho,Slava Berger,Carla Freire,Lenise J Kim,Mi-Kyung Shin,Stone R Streeter,Nishitha Hosamane,Meaghan E Cabassa,Frederick Anokye-Danso,Olga Dergacheva,Mateus R Amorim,Thomaz Fleury-Curado,Jonathan C Jun,Alan R Schwartz,Rexford S Ahima,David Mendelowitz,Vsevolod Y Polotsky

Journal of neuroinflammation 18:26 PubMed33468172

2021

Activation of MC1R with BMS-470539 attenuates neuroinflammation via cAMP/PKA/Nurr1 pathway after neonatal hypoxic-ischemic brain injury in rats.

Applications

Unspecified application

Species

Unspecified reactive species

Shufeng Yu,Desislava Met Doycheva,Marcin Gamdzyk,Yijun Yang,Cameron Lenahan,Gaigai Li,Dujuan Li,Lifei Lian,Jiping Tang,Jun Lu,John H Zhang
View all publications

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